Dr. Andreas Hentschel

Journal of Neurology, Vol. 273, No. 2, 2026, P. 94

Mroczek M, Preusse C, Hentschel A, Chroscinska-Krawczyk M, Bielak M, Sobolewska A, Della Marina A, Hila A, Iyadurai S, Kraft F, Chetty VK, Muhmann D,…

Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers

Clinical Genetics, Vol. 2026, No. 5, 2026, P. 978-983

Kilicarslan OA, Gangfuß A, Hentschel A, Koelbel H, Muhmann D, Töpf A, Stöhr M, Chen L, Horvath R, Thompson R, Schara-Schmidt U, Kurth I, Lochmüller…

A Homozygous CPSF1 Variant Causes Congenital Cataract, Intellectual Disability and Hyperphagia

Journal of Clinical Medicine, Vol. 14, No. 24, 2025

Aksel Kilicarslan O, Gangfuss A, Kolbel H, Muhmann D, Polavarapu K, Thompson R, Schmitt L, Lessard L, Chen L, Eisenkolbl A, Schara-Schmidt U,…

Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report

Journal of Proteome Research, Vol. 2025, 2025, P. 484-490

Lange E, Schallert K, Schwerdt J, Ghosh S, Hentschel A, Reinders Y, Heyer R.

The Omics Molecule Extractor: A Web Application for the Selection of Potential Biomarker Panels

Journal of Neuropathology and Experimental Neurology, Vol. 85, No. 4, 2025, P. 351-362

Merlet AN, Lacene E, Nelson I, Brochier G, Labasse C, Chanut A, Madelaine A, Beuvin M, Bonne G, Feasson L, Minot M, Noury J, Fradin M, Savarese M,…

Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA)

Acta Neuropathologica, Vol. 2025, No. 1, 2025

Stascheit F, Roos A, Schroeter CB, Thomas JK, Hahn K, Preßler H, Hentschel A, Schlotter-Weigel B, Schoser B, Ruck T, Meisel A, Stenzel W, Preusse C.

Complement profiling of sural nerves in chronic inflammatory demyelinating polyneuropathy